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Selectivity improvement in protein nanopatterning with a hydroxy-terminated self-assembled monolayer template

机译:羟基端接的自组装单层模板提高蛋白质纳米图案的选择性

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摘要

Protein nanopatterning techniques to fulfil the requirement for reducing nonspecific adsorption are demonstrated. A target protein is selectively immobilized on a hydroxy-terminated self-assembled monolayer template, the pattern of which is modified with streptavidin used as the intermediating molecule. 3-aminopropyltrimethoxysilane (APTES) used as the intermediating molecule induces nonspecific adsorption of proteins due to nonspecific adsorption of APTES itself. The data indicate that reducing nonspecific adsorption of both the target protein and the intermediating molecule is important for selectivity improvement in protein patterning. As a result of the refinement, a protein nanopattern of 250 nm in diameter has been fabricated.
机译:蛋白质纳米图案技术可以满足减少非特异性吸附的要求。将靶蛋白选择性地固定在羟基末端的自组装单层模板上,该模板的图案被链霉亲和素用作中间分子修饰。由于APTES本身的非特异性吸附,用作中间分子的3-氨基丙基三甲氧基硅烷(APTES)诱导了蛋白质的非特异性吸附。数据表明,减少靶蛋白和中间分子的非特异性吸附对于提高蛋白构图的选择性很重要。作为改进的结果,已经制造了直径为250nm的蛋白质纳米图案。

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